FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
SYS*STIM 220
K Number: K883080
·
Decision Apr 27, 1989
Classifications
1
FEI Numbers
46
Registration Numbers
46
Same Product Code
72
Applicant Total
32
Review Days
280
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Basic Information
- Device Name
- SYS*STIM 220
- K Number
- K883080
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 882.5890
- Medical Specialty
- Neurology
- Decision
- Substantially Equivalent
- Applicant
- Mettler Electronics Corp.
- Date Received
- July 21, 1988
- Decision Date
- April 27, 1989
- Product Code
- LIH
- Advisory Committee
- Neurology
- Review Advisory Committee
- NE
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| LIH | Interferential Current Therapy | FDA class 2 | Neurology |
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